• ALBA CONECET: Get a Job!

    ປະກາດການໂຄສະນາການຈ້າງງານຟຣີ -ການລະບາດຂອງພະຍາດໂຄວິດ-19 ໃນທົ່ວໂລກໄດ້ຂັດຂວາງການພັດທະນາເສດຖະກິດ ແລະ ການຈ້າງງານຫຼຸດລົງ. ໂຄງການ ALBA Connect ມີຈຸດປະສົງເພື່ອຊ່ວຍໃຫ້ພະນັກງານໃນລາວຊອກຫາໂອກາດວຽກເຮັດງານທຳໃນອຸດສາຫະກຳການຢາ. ພວກເຮົາຈະໂຄສະນາໂຄງການອອນໄລນ໌ແລະໃນຕົວເມືອງ, ໂດຍສະເພາະພວກເຮົາຈະລົງໂຄສະນາແລະໂປສເຕີໃນມະຫາວິທະຍາໄລ, ເມືອງທຸລະກິດ. ເງື່ອນໄຂການເຂົ້າຮ່ວມໂຄງການ ສະຖາບັນທີ່ເຂົ້າຮ່ວມຕ້ອງຕອບສະຫນອງເງື່ອນໄຂພື້ນຖານຕໍ່ໄປນີ້ໃນເວລາດຽວກັນ. ຮັບສະເພາະສິ່ງພິມຈາກສະຖາບັນ ປະຈຸບັນການປະກາດຮັບສະໝັກວຽກຈາກອົງການ ຫຼື ອົງການຈັດຕັ້ງໃນຂະແໜງອຸດສາຫະກຳການແພດ ແລະ ຮ້ານຂາຍຢາ. ປະກາດຮັບສະໝັກວຽກແມ່ນໄດ້ຜ່ານ: [HR-Nith] ຢູ່ໃນ [ຊ່ອງທາງວຽກ] ຂອງ lienTeh. ປະເພດອົງການຈັດຕັ້ງ ສະຖາບັນການແພດ: ໂຮງຮຽນການແພດ, ໂຮງຫມໍ, ຄລີນິກ, ໂຮງງານຜະລິດຢາ, ຮ້ານຂາຍຢາ, ບໍລິສັດການຄ້າ, ແລະອື່ນໆ. ທີມ​ກູ້​ໄພ​: ທີມ​ງານ​ກູ້​ໄພ​ການ​ແພດ​ແລະ​ທີມ​ກູ້​ໄພ​ມື​ອາ​ຊີບ​ອື່ນໆ​. ອົງການຈັດຕັ້ງອື່ນໆ: ເຊັ່ນ: ສະມາຄົມອຸດສາຫະກໍາຢາ, ແລະອື່ນໆ. ຂໍ້ມູນວຽກ 1. ໂລໂກ້ຂອງບໍລິສັດຮັບສະໝັກພະນັກງານ. 2. ເອກະສານລະອຽດໃນການສະໝັກຕໍາແໜ່ງງານ. 3. ຂໍ້ມູນຕິດຕໍ່ HR ຂອງບໍລິສັດຮັບສະໝັກ.…

  • Ronapreve Approved for Additional Indication as a Preventive Treatment of Symptomatic COVID-19 in Japan

    TOKYO, November 5, 2021 Chugai Pharmaceutical Co., Ltd. (TOKYO: 4519) announced that it obtained approval from the Ministry of Health, Labour and Welfare (MHLW) for the anti-SARS-CoV-2 monoclonal antibody RONAPREVE® [generic name: casirivimab (genetical recombination) /imdevimab (genetical recombination)] for the additional indication of the prevention of symptomatic SARS-CoV-2 infection (COVID-19). The Special…

  • Bronchitol(Mannitol)approved in Swissin for treat Cystic Fibrosis

    FREIENBACH, Switzerland–04.11.2021 EffRx Pharmaceuticals SA, a commercial-stage company that commercializes niche and orphan medicines in Switzerland and Europe, today announced that Swissmedic has approved Bronchitol® (inhaled mannitol) for the treatment of cystic fibrosis (CF) in adults and in children aged 6 years and above as add‐on to other medicines. The clinical…

  • LAGEVRIO (Molnupiravir) approved in U.K. for the Treatment of Mild-to-Moderate COVID-19 in Adults

    KENILWORTH, N.J. & MIAMI--November 4, 2021 Merck (NYSE: MRK), known as MSD outside the United States and Canada, and Ridgeback Biotherapeutics today announced that the United Kingdom Medicines and Healthcare products Regulatory Agency (MHRA) has granted authorization in the United Kingdom (U.K.) for molnupiravir (MK-4482, EIDD-2801), the first oral antiviral…

  • Ozawade (pitolisant) approved by EMA for the treatment of excessive daytime sleepiness (EDS) associated with obstructive sleep apnoea (OSA) in adults

    28th October 2021 The European Medicines Agency (EMA) has approved Bioprojet’s Ozawade (pitolisant) for the treatment of excessive daytime sleepiness (EDS) associated with obstructive sleep apnoea (OSA) in adults. Ozawade was evaluated in two Phase III clinical studies in the treatment of EDS in patients suffering from OSA – HAROSA…

  • Libtayo(Cemiplimab) approved in Canada for locally advanced basal cell carcinoma (BCC) patients

    MISSISSAUGA, ON, Oct. 29, 2021  Libtayo® (cemiplimab) is now approved in Canada for the treatment of adults with locally advanced basal cell carcinoma (BCC) previously treated with a hedgehog pathway inhibitor (HHI).The approval of Libtayo follows the European Commission (EC) approval announced in June 2021 and the US in February 2021. With today's announcement, Libtayo is now offered as…

  • VUITY™ (pilocarpine HCI ophthalmic solution) 1.25% is approved by FDA to treat Presbyopia (Age-Related Blurry Near Vision)

    NORTH CHICAGO, USA., Oct. 29, 2021 Allergan, an AbbVie (NYSE: ABBV) company, announced the U.S. Food and Drug Administration (FDA) approval of VUITY™ (pilocarpine HCl ophthalmic solution) 1.25% for the treatment of presbyopia, commonly known as age-related blurry near vision, in adults. VUITY is the first and only FDA-approved eye drop to treat this…

  • Scemblix® (asciminib) is approved in USA for the treatment of chronic myeloid leukemia

    Basel, October 29, 2021 Novartis announced today that the US Food and Drug Administration (FDA) approved Scemblix® (asciminib) for the treatment of chronic myeloid leukemia (CML) in two distinct indications. The FDA granted Scemblix accelerated approval for adult patients with Philadelphia chromosome-positive CML in chronic phase (Ph+ CML-CP) previously treated with…

  • KEYTRUDA (pembrolizumab) Plus Chemotherapy as Treatment is approved in European for Certain Patients With Locally Recurrent Unresectable or Metastatic Triple-Negative Breast Cancer (TNBC)

    KENILWORTH, N.J.--October 22, 2021  Merck (NYSE: MRK), known as MSD outside the United States and Canada, announced that the European Commission (EC) has approved KEYTRUDA, Merck’s anti-PD-1 therapy, in combination with chemotherapy for the first-line treatment of locally recurrent unresectable or metastatic triple-negative breast cancer (TNBC) in adults whose tumors…

  • Ryeqo is approved in UK for the treatment of moderate to severe symptoms of uterine fibroids in adult women of reproductive age

    London, United Kingdom, Tuesday 26 October 2021 Gedeon Richter UK Ltd. (“Gedeon Richter”) today announced that the Medicines and Healthcare Products Regulatory Agency (MHRA) has granted a licence for Ryeqo (relugolix 40 mg, estradiol 1 mg, and norethisterone acetate 0.5 mg – herein “relugolix combination therapy”), for the treatment of…


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